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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170768Generated: November 2, 2026

Sodium borohydride → 1-(4-(3-Bromopropyl)phenyl)ethanol

https://huagongshe.com/reaction/1170768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-Acetylphenyl)-3-bromopropaneHCID 14817035—
SolventMethanolHCID 887—
Product1-(4-(3-Bromopropyl)phenyl)ethanolHCID 67523991—

Reaction Steps

Also disclosed herein is a method of making 4-vinylbenzenepropanethiol. The method includes providing 1-bromo-3-phenylpropane, adding acetic anhydride and aluminum chloride, incubating the mixture at from about −20 to about 20 degrees Celsius for from about 1 hour to about 12 hours, isolating the resulting p-(3-bromopropyl)acetophenone, adding sodium borohydride to the p-(3-bromopropyl)acetophenone solution in methanol, incubating the mixture at about 0 degrees Celsius for about 2 hours, isolating the resulting p-(3-bromopropyl)-α-methylbenzenemethanol, adding toluensulfonic acid to the solution of p-(3-bromopropyl)-α-methylbenzenemethanol in toluene, refluxing the mixture under inert atmosphere for about 4 hours, isolating the resulting p-(3-Bromopropyl)styrene, adding thiourea to the p-(3-Bromopropyl)styrene, gently refluxing the mixture for about 16 hours, adding sodium hydroxide, and gently refluxing the mixture for about 4 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829155B1
Source datasetuspto-grants-2010_11
ORD IDord-1107a1ba0ee2402cbeeb9d3848505015
Source noteuspto-grants-2010_11